TY - JOUR
T1 - Targeted therapies for ER+/HER2- metastatic breast cancer
AU - Yamamoto-Ibusuki, Mutsuko
AU - Arnedos, Monica
AU - André, Fabrice
N1 - Publisher Copyright:
© 2015 Yamamoto-Ibusuki et al.
PY - 2015/12/12
Y1 - 2015/12/12
N2 - The majority of breast cancers present with estrogen receptor (ER)-positive and human epidermal growth factor receptor (HER2)-negative features and might benefit from endocrine therapy. Although endocrine therapy has notably evolved during the last decades, the invariable appearance of endocrine resistance, either primary or secondary, remains an important issue in this type of tumor. The improvement of our understanding of the cancer genome has identified some promising targets that might be responsible or linked to endocrine resistance, including alterations affecting main signaling pathways like PI3K/Akt/mTOR and CCND1/CDK4-6 as well as the identification of new ESR1 somatic mutations, leading to an array of new targeted therapies that might circumvent or prevent endocrine resistance. In this review, we have summarized the main targeted therapies that are currently being tested in ER+ breast cancer, the rationale behind them, and the new agents and combinational treatments to come.
AB - The majority of breast cancers present with estrogen receptor (ER)-positive and human epidermal growth factor receptor (HER2)-negative features and might benefit from endocrine therapy. Although endocrine therapy has notably evolved during the last decades, the invariable appearance of endocrine resistance, either primary or secondary, remains an important issue in this type of tumor. The improvement of our understanding of the cancer genome has identified some promising targets that might be responsible or linked to endocrine resistance, including alterations affecting main signaling pathways like PI3K/Akt/mTOR and CCND1/CDK4-6 as well as the identification of new ESR1 somatic mutations, leading to an array of new targeted therapies that might circumvent or prevent endocrine resistance. In this review, we have summarized the main targeted therapies that are currently being tested in ER+ breast cancer, the rationale behind them, and the new agents and combinational treatments to come.
KW - Breast cancer
KW - Cancer genome
KW - Endocrine therapy resistance
KW - Targeted therapy
UR - http://www.scopus.com/inward/record.url?scp=84938983229&partnerID=8YFLogxK
U2 - 10.1186/s12916-015-0369-5
DO - 10.1186/s12916-015-0369-5
M3 - Review article
C2 - 26059247
AN - SCOPUS:84938983229
SN - 1741-7015
VL - 13
JO - BMC Medicine
JF - BMC Medicine
IS - 1
M1 - 137
ER -